Expresso® Rhamnose SUMO Cloning and Expression System,Expresso® Rhamnose SUMO克隆及蛋白表达系统
货号:49013-1 ,49013-2
规格:5 rxns,10 rxns
价格:4036,7208
产品类型:PCR 及DNA聚合酶
品牌:Lucigen
The Expresso Rhamnose Cloning and Protein Expression Systems are designed for fast, easy, and efficient directional cloning and expression of PCR-amplified genes using Expressioneering Technology. Expressioneering Technology usesin vivohomologous recombination to seamlessly clone PCR amplified DNA into specially designed expression vectors without the need for enzymes or purification steps. A single host strain is used for both stable cloning and controlled protein expression, making Expresso Rhamnose the fastest cloning and expression systems available. The systems come complete with pre-processed expression plasmids and competent cells, supplied in single transformation vials. |
优点: |
▪Five-second, directional, enzyme-free PCR cloning! 90% recombinants.▪Single competent cell host strain for both cloning and expression.▪Tighter expression control with tunable Rhamnose (rhaPBAD) promoter. |
数据: |
Figure 1. Expressioneering Technologyusesin vivohomologous recombination to seamlessly clone PCR amplified DNA into specially designed expression vectors without the need for enzymes or purification steps. The desired insert is simply amplified with primers that include 18 bases that overlap with the ends of the Expresso® vector. The unpurified PCR amplicon is then mixed with the pRham expression plasmid and the high-efficiency competent cells provided, and directly plated on appropriate media.Figure 2.pRham expression vectors.RBS, ribosome binding site; ATG, translation start site; Stop, translation end site; Kan, kanamycin resistance gene; ROP, Repressor of Priming (for low copy number); Ori, origin of replication. CloneSmart® transcription terminators (T) prevent transcription into or out of the insert, and a terminator follows the cloning site. The 6xHis affinity tag is fused to the amino terminus (pRham N-His) or at the carboxyl terminus (pRham C-His) of the expressed target protein. Also available: pRham N-His SUMO Vector for enhanced soluble protein expression with cleavable SUMO solubility tag.Figure 3. Tuning recombinant protein expression levels with rhamnose induction.The pRham C-His Kan Vector containing a gene encoding a blue fluorescent protein (BFP) was transformed intoE. cloni10G cells. An uninduced starter culture was inoculated to a starting OD600 of 0.8 into culture tubes containing LB media with 30 µg/ml kanamycin and the indicated concentrations of rhamnose (0 to 0.2% w/v) or 2% glucose. After overnight incubation at 37°C, samples were harvested by centrifugation, lysed in SDS-PAGE loading buffer, and analyzed by SDS-PAGE. The Coomassie-blue stained gel shows total cellular protein. Protein expression levels are responsive to rhamnose concentrations between 0.001% and 0.2%. |
相关产品: |
▪Expresso® Rhamnose Cloning and Expression System, N-His(货号#49011)▪ Expresso® Rhamnose Cloning and Expression System, C-His(货号#49012)▪Glucose Solution, 15% w/v(货号#49022)▪Rhamnose Solution, 20% w/v(货号#49021)▪SUMO Express Protease(货号#30801) |
技术参数 产品优点 - Enzyme-free directional PCR cloning in seconds! - Save days of effort with ready-to-use vectors and competent cells - NO ligation step. - Tightly-controlled expression of N-terminal 6xHis-tagged proteins with cleavable SUMO solubility tag. - Systems available with expression under the control of T7 or tunable Rhamnose promoters.
产品应用 The Expresso SUMO Cloning and Protein Expression Systems are designed for fast, easy, and efficient directional cloning and soluble expression of PCR-amplified genes.
组成成分 The Expresso T7 SUMO Cloning and Expression System contains pre-processed pETite® N-His SUMO Vector DNA, HI-Control™ 10G Chemically Competent Cells for cloning, and HI Control BL21(DE3) Chemically Competent Cells for protein expression. Also included are SUMO Positive Control C Insert DNA, transformation positive control pUC DNA, SUMO Express Protease, SUMO Cleavage Control Protein, and forward and reverse PCR primers to confirm clones.
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